Symmetry LEKSELL 53-1126

GUDID 00887482021804

LAMINECTOMY RONGEUR FULL WIDE

SYMMETRY SURGICAL INC.

Rib rongeur

• Primary Device ID: 00887482021804
• NIH Device Record Key: aa3e77f2-4957-493b-8c2b-1cdb43504761
• Commercial Distribution Discontinuation: 9999-01-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Symmetry LEKSELL
• Version Model Number: 53-1126
• Catalog Number: 53-1126
• Company DUNS: 079641356
• Company Name: SYMMETRY SURGICAL INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887482021804 [Primary]

FDA Product Code

• HAE: Rongeur, Manual

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00887482021804]

Moist Heat or Steam Sterilization

[00887482021804]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-07-12
• Device Publish Date: 2016-05-20

On-Brand Devices [Symmetry LEKSELL]

• 00887482036662: Rongeur Regular Curve
• 00887482021828: LAMINECTOMY RONGEUR FULL NARR
• 00887482021811: LAMINECTOMY RONGEUR REG NARR
• 00887482021804: LAMINECTOMY RONGEUR FULL WIDE
• 00887482021798: LAMINECTOMY RONGEUR REG WIDE